Product NDC: | 63629-1675 |
Proprietary Name: | Allopurinol |
Non Proprietary Name: | Allopurinol |
Active Ingredient(s): | 100 mg/1 & nbsp; Allopurinol |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63629-1675 |
Labeler Name: | Bryant Ranch Prepack |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018832 |
Marketing Category: | NDA |
Start Marketing Date: | 20090406 |
Package NDC: | 63629-1675-2 |
Package Description: | 30 TABLET in 1 BOTTLE (63629-1675-2) |
NDC Code | 63629-1675-2 |
Proprietary Name | Allopurinol |
Package Description | 30 TABLET in 1 BOTTLE (63629-1675-2) |
Product NDC | 63629-1675 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Allopurinol |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20090406 |
Marketing Category Name | NDA |
Labeler Name | Bryant Ranch Prepack |
Substance Name | ALLOPURINOL |
Strength Number | 100 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA] |